A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975163



Internal ID18610371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:26588421..26598720hg38UCSC Ensembl
Innerchr11:26609968..26620267hg19UCSC Ensembl
Innerchr11:26566544..26576843hg18UCSC Ensembl
Cytoband11p14.2
Allele length
AssemblyAllele length
hg3810300
hg1910300
hg1810300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1880555, nssv1880556, nssv1880560, nssv1880561, nssv1880557, nssv1880562, nssv1880564, nssv1880563, nssv1880559, nssv1880558
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesANO3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975163
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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